Proteck, Inc.
Country not established
- Devices
- 1
What Proteck, Inc. makes
Proteck, Inc. manufactures a straight stem femoral head prosthesis, a component used in hip replacement surgeries to restore joint function.
The company’s product is classified as a Class II medical device in the US and is listed under the FDA’s 510(k) pathway. The manufacturer is based in the United States.
Catalogue
Straight Stem Femoral Head Prosthesis Ref K831851
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Proteck, Inc. have in the registry?
The registry currently lists 1 device for Proteck, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Proteck, Inc.'s devices?
Among its 1 most recently registered device, Proteck, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Proteck, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Proteck, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Proteck, Inc. in the registry?
The most recently registered devices listed for Proteck, Inc. include STRAIGHT STEM FEMORAL HEAD PROSTHESIS.